A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887165



Internal ID22662157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47935641..47935892hg38UCSC Ensembl
chr2:48162780..48163031hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887165
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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